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(E)-METHYL-ENDO-(8'-METHYL-1',4',4A',9A'-TETRAHYDRO-1',4'-METHANO-9H-FLUOREN-9'-YLIDENE)-ETHANOATE

Compound with spectra: 2 NMR

(E)-METHYL-ENDO-(8'-METHYL-1',4',4A',9A'-TETRAHYDRO-1',4'-METHANO-9H-FLUOREN-9'-YLIDENE)-ETHANOATE
SpectraBase Compound ID wnKS6QVicX
InChI InChI=1S/C18H18O2/c1-10-4-3-5-13-16(10)14(9-15(19)20-2)18-12-7-6-11(8-12)17(13)18/h3-7,9,11-12,17-18H,8H2,1-2H3/b14-9-/t11-,12+,17+,18-/m0/s1
InChIKey XHINHSCSMQPATF-SURSLFJRSA-N
Mol Weight 266.34 g/mol
Molecular Formula C18H18O2
Exact Mass 266.13068 g/mol
Enantiomer InChIKey XHINHSCSMQPATF-YFFRLWMBSA-N

View Spectrum of (E)-METHYL-ENDO-(8'-METHYL-1',4',4A',9A'-TETRAHYDRO-1',4'-METHANO-9H-FLUOREN-9'-YLIDENE)-ETHANOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (E)-METHYL-ENDO-(8'-METHYL-1',4',4A',9A'-TETRAHYDRO-1',4'-METHANO-9H-FLUOREN-9'-YLIDENE)-ETHANOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (Z)-METHYL-ENDO-(8'-METHYL-1',4',4A',9A'-TETRAHYDRO-1',4'-METHANO-9H-FLUOREN-9'-YLIDENE)-ETHANOATE
(Z)-methyl endo-(8'-methyl-1',4',4'a,9'a-tetrahydro-1',4'-methano-9'H-fluoren-9'-ylidene)ethanoate
(E)-endo-(8'-methyl-1',4',4'a,9'a-tetrahydro-1',4'-methano-9'H-fluoren-9'-ylidene)ethanoic acid
(Z)-endo-(8'-methyl-1',4',4'a,9'a-tetrahydro-1',4'-methano-9'H-fluoren-9'-ylidene)ethanoic acid
ENDO-(E)-(8'-METHYL-1',4',4A',9A'-TETRAHYDRO-1',4'-METHANO-9H-FLUOREN-9'-YLIDENE)-ETHANOIC-ACID
11H-dihydrobicyclo[2.2.1]hepteno[b]cyclopent[4,5-a]azulen-11-one
1H-benz[f]isoindole-1,3(2H)-dione, 2-(3-hydroxyphenyl)-4-phenyl-
.gamma.-Lactone of 18-hydroxydeoxycortexone
(2R,2aS,8bS)-1,2,2a,8b-Tetrahydro-2-morpholino-cyclobuta[a] naphthalene2,8b-dicarbonitrile
(2R,2aS,8bR)-1,2,2a,8b-Tetrahydro-2-morpholino-cyclobuta[a] naphthalene2,8b-dicarbonitrile
3',4'-DIHYDROXY-6'',6'',6''',6'''-TETRAMETHYLBIS-(PYRANO-[2'',3'':5,6:2''',3''':7,8]-ISOFLAVONE
Title Journal or Book Year
The 1,2-Didehydronaphthalene to 1H-Indenylidenecarbene Rearrangement: Formation of 7-Methyl-1H-Indenylideneethenone and Its Rearrangement to Acenaphthylen-4-Ol in a Flash Vacuum Pyrolytic Reaction Australian Journal of Chemistry 1987

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